Canonical Allele Identifier: PA2827981067
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 646270
ClinVar RCV Id: RCV003535915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2635Glu
CA16038683
NM_001354899.2:c.7905C>A
CA16038684
NM_001354899.2:c.7905C>G